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Lead the clinical development of pharmaceutical compounds and delivering technology to meet business needs.Specialties: Leading IT projects (web development, clinical trials), Systems Support, Clinical Trial Data Delivery, Drug Registration Process
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Senior Director - Real World Evidence CoeEli Lilly And Company Feb 2022 - PresentIndianapolis, Indiana, Us -
Director Of Information Technology - Clinical ResearchEli Lilly And Company Jun 1986 - Feb 2022Indianapolis, Indiana, Us -
Director, Real World DataEli Lilly And Company Jun 1986 - Feb 2022Indianapolis, Indiana, UsI am responsible acquisition and management of Real World Data used across Lilly for secondary research to gain insights into the patient experience on our medicines. Capabilities my team is responsible for are as follows: acquisition of new data sources, enhancing current data sources, deliver tools to interact with the data, and to effectively manage loading and access to data.
Greg Cunningham Skills
Greg Cunningham Education Details
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Ball State UniversityComputer Science -
Roncalli High School
Frequently Asked Questions about Greg Cunningham
What company does Greg Cunningham work for?
Greg Cunningham works for Eli Lilly And Company
What is Greg Cunningham's role at the current company?
Greg Cunningham's current role is Senior Director.
What is Greg Cunningham's email address?
Greg Cunningham's email address is cu****@****lly.com
What is Greg Cunningham's direct phone number?
Greg Cunningham's direct phone number is +131727*****
What schools did Greg Cunningham attend?
Greg Cunningham attended Ball State University, Roncalli High School.
What are some of Greg Cunningham's interests?
Greg Cunningham has interest in Family, Clinical Trial Databases, Clinical Trials, Health Care Databases, Web Development, Leading Information Technology Projects, Competitive Distance Running, Personal, Regulatory Submissions (Fda), Sas Software Tools.
What skills is Greg Cunningham known for?
Greg Cunningham has skills like Clinical Trials, Clinical Data Management, Pharmaceutical Industry, Clinical Development, Fda, Computer System Validation, Regulatory Submissions, 21 Cfr Part 11, Protocol, Oncology, Gcp, Cro.
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